Systems and methods for production and separation of hydrogen and carbon dioxide

ABSTRACT

The present disclosure relates to systems and methods useful for providing one or more chemical compounds in a substantially pure form. In particular, the systems and methods can be configured for separation of carbon dioxide from a process stream, such as a process stream in a hydrogen production system. As such, the present disclosure can provide systems and method for production of hydrogen and/or carbon dioxide.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims priority to U.S. Provisional PatentApplication No. 62/583,816, filed Nov. 9, 2017, and U.S. ProvisionalPatent Application No. 62/670,175, filed May 11, 2018, the disclosuresof which are incorporated herein by reference.

FIELD OF THE INVENTION

The present disclosure provides systems and methods for producingmaterials that are typically gaseous at standard temperature andpressure, such as hydrogen and carbon dioxide. In particular, thepresent disclosure provides for separation of carbon dioxide from anindustrial process stream, and specifically from a process stream thatfurther includes hydrogen.

BACKGROUND

Hydrogen has long been viewed as a desirable energy source because ofits clean combustion characteristics producing only water. Hydrogen canbe produced from hydrocarbon fuels with capture of CO₂ avoiding any CO₂emission to the atmosphere. Hydrogen can be a desirable commodity foruse in fuel cells (particularly in vehicle production), heatingapplications, oil refining, fertilizer production, and other chemicalproduction. For example, hydrogen can be used as a fuel for electricvehicle propulsion using fuel cells advantageously coupled to highcapacity electric storage batteries. Beneficially, use of hydrogen as afuel can eliminate CO₂, NOx, CO, and hydrocarbon emissions and thussignificantly reduce air pollution particularly at ground level in largeurban conurbations. Any path to implementation of a hydrogen-based worldeconomy, however, would require a very large hydrogen productioncapacity. Moreover, such hydrogen production method would need to becapable of achieving simultaneously low hydrogen production costtogether with the capture of near 100% of the CO₂ and other impuritiesderived from any carbonaceous or hydrocarbon fuel utilized.

Hydrogen use as a fuel source can also be beneficial to reduce oreliminate carbon dioxide emissions associated with more conventionalpower production processes. For example, hydrogen can be diluted withnitrogen and/or steam and used as the fuel in a gas turbine combinedcycle power generation system.

Gas turbine combined cycle power generation systems are a major sourceof electrical power generation worldwide because of their ability toproduce power from natural gas with an efficiency in the range of 55% to62%, on a lower heating value (LHV) basis. Despite the desirableefficiency, such systems are still problematic since the carbon in thefuel is emitted to the atmosphere as carbon dioxide. To overcome thisproblem and capture the CO₂ derived from fuel combustion a number ofpossibilities have been suggested. It is possible to operate the gasturbine with CO₂ in place of air as the working fluid by recycling theturbine exhaust back to the gas turbine compressor inlet followingcooling to generate steam for additional power production. The fuel forthe gas turbine is burned with pure oxygen in an oxy-fuel burner so thatall atmospheric nitrogen is eliminated from the closed cycle system andCO₂ becomes the working fluid in the gas turbine. The product CO₂derived from fuel combustion together with condensed water are removedupstream of the inlet of the gas turbine compressor section. Chemicaland/or physical solvent scrubbing processes can be used to treat the gasturbine exhaust to remove CO₂. As discussed above, it is possible toeliminate the emissions of CO₂ and other fuel and combustion derivedpollutants from the gas turbine exhaust by utilizing hydrogen as thefuel in the gas turbine. This approach requires a consistent high volumelow cost hydrogen source that is preferentially provided from a systemin which substantially all the CO₂ and other fuel or combustion derivedimpurities are removed for separate disposal. Hydrogen production inexcess of that required for gas turbine fuel can be provided from such asystem for use in the wider applications for hydrogen as a fueldescribed above.

Other industrial processes are also known that utilize significantamounts of hydrogen gas while also being significant emitters of CO₂.Modern refineries, for example, utilize (on average) approximately 250scf of H₂ per barrel of oil that is processed. Steam methane reforming(SMR), which is the main process currently being used for H₂ generation,has a CO₂ intensity of 24.5 kg-CO₂/kscf-H₂ which results in 6.1 kg-CO₂being emitted per barrel of oil processed, this amount being attributedsolely to the use of H₂ in hydrotreating/hydrocracking processes. Theoverall CO₂ emission per barrel is higher than this and ranges from6.5-33 kg-CO₂/barrel of oil processed.

Much of the world's power is derived from the combustion of coal insteam cycle power plants. Methods of CO₂ removal from a power boilerinclude coal combustion with pure oxygen in an oxy-fuel burner dilutedwith recycle flue gas so that nitrogen is largely eliminated from thesystem and net CO₂ product derived from the coal can be produced fordisposal. Alternatively the stack gas can be treated with limestoneslurry to remove sulfur dioxide followed by the removal of CO₂ from thestack gas using an amine chemical scrubbing process.

A further method of using coal or other solid or heavy liquid fuels suchas refinery waste products or biomass is to gasify the fuels using pureoxygen in a partial oxidation reactor followed by gas treating toconvert CO by reaction with steam in a catalytic reactor giving hydrogenand CO₂ then removal of CO₂ and sulfur compounds and other traceimpurities giving a substantially pure hydrogen product for use as cleanfuel in a combined cycle gas turbine power generation system.

A further method of power generation using natural gas, coal, refinerywaste, or biomass fuel would involve the use of a closed cycle highpressure oxy-fuel power generation system using a working fluid, such asCO₂, N₂, Helium, H₂O, or the like. For example, systems utilizing N₂ asthe working fluid are described in U.S. Pat. Nos. 9,410,481 and9,611,785, the disclosures of which are incorporated herein byreference.

In light of the significant amounts of CO₂ produced in variousindustrial gas streams, such as those exemplified above, there is a needfor various processes for CO₂ removal from process streams. Separationand purification of carbon dioxide from industrial waste gas streams isa challenging process due to high energy and equipment costs. Currently,climate change due to global warming is an existential threat tohumanity and release of significant amount of carbon dioxide to theatmosphere due to human activities (industry, transportation,residential, etc.) has been known as the main reason behind it. Thus,development of novel and efficient ways to capture and sequester orreuse the CO₂ emission from various industrial processes is of paramountimportance. For example, global hydrogen generation capacity in 2017 wasabout 65M metric tons, and about 99% of that amount was produced throughprocesses that release about 0.74 Gt/year of CO₂ into the atmosphere.This was more than 2% of overall global CO₂ emission in 2017 which wasonly due to hydrogen generation.

Known methods for removal of carbon dioxide from gas streams includeabsorption of carbon dioxide using a chemical solvent such as an aminesolution of a physical solvent such as the Selexol™ process, separationusing membrane diffusion, and separation using adsorption on a solidadsorbent, such as a zeolite or activated carbon. Fuel gas streamscontaining CO₂ are often burned releasing CO₂ into the atmosphere, andknown methods for separation of CO₂ from gas streams are recognized asbeing prohibitively costly. Accordingly, there is a need for lower costCO₂ removal systems which can easily be integrated into existingprocesses such as hydrogen generation, capable of 100% CO₂ recovery.

Hydrogen production systems using any hydrocarbon or carbonaceous fuelwill in general require a large quantity of high temperature heat (e.g.,about 500° C. to about 1000° C.) for feed preheating, and they producelarge quantities of excess heat at low temperatures (e.g., about 200° C.to about 400° C.). Power stations have high grade heat available, andthey can utilize low grade heat integrated into their systems. Becauseof the desirability of the use of hydrogen as a fuel source, thereremains a need for means to provide hydrogen fuel at a low costsubstantially without CO₂ emission to the atmosphere.

Previous efforts have been undertaken to provide for combined productionof hydrogen and carbon dioxide, such as disclosed in U.S. Pat. No.8,021,464. Such methods, however, and lacking in simplicity and costefficiency. Accordingly, there remains a need for further systems andmethods for removing carbon dioxide from process streams as well assimultaneously producing a valuable hydrogen stream.

SUMMARY OF THE INVENTION

The present disclosure relates to systems and methods for providing oneor more streams of a substantially pure chemical compound, such ashydrogen and/or carbon dioxide. The disclosed systems and methodsbeneficially utilize an auto-refrigeration system that efficientlyseparated carbon dioxide from an industrial process stream at reducedcost. As such, in some embodiments, the present disclosure particularlycan provide systems and methods for production of a carbon dioxidestream, specifically through separation of the carbon dioxide from anindustrial stream including carbon dioxide and at least one furthermaterial. Such carbon dioxide separation can be particularly beneficialfor use with systems and methods that produce a stream comprisinghydrogen and carbon dioxide. Accordingly, in some embodiments, thepresent disclosure particularly can provide systems and methods forproduction of substantially pure hydrogen gas, such systems and methodsinclude removal of carbon dioxide from a crude hydrogen product stream,such as through the auto-refrigeration methods described further herein.

Hydrogen production can comprise partially oxidizing or reacting ahydrocarbon fuel with oxygen in the presence of steam and or CO₂ toprovide gaseous products that include and/or are converted intohydrogen. Moreover, because of the ability to efficiently remove CO₂ ata significantly reduced cost, the hydrogen can be produced withsubstantially zero CO₂ and other impurity emissions, and the hydrogencan be produced in a substantially pure form so that it can be utilizedin a variety of manners, such as being use as a vehicle fuel, being usedfor power production or for heating, being used for production offertilizer or other chemicals, or being used in oil refining.

In some embodiments the present disclosure can include the production ofa mixture of H₂+CO using a single stage catalytic reactor with steamplus natural gas feeds, such as via steam methane reforming (SMR).Alternatively H₂+CO can be produced by the partial oxidation of agaseous or liquid or solid hydrocarbon or carbonaceous fuel using pureoxygen (PDX) or from a catalytic auto-thermal reactor (ATR) using agaseous or liquid hydrocarbon fuel with O₂ plus steam feed. In somepreferred embodiments, the present disclosure further can relate tosystems and methods for generation of H₂+CO in a PDX or ATR reactorfollowed by the use of a gas heated reformer (GHR) in either a series orparallel mode to the PDX or ATR reactor to produce additional H₂ and CO(i.e., synthesis gas) by utilizing the exhaust sensible heat in the PDXand/or ATR reactor system to provide the heat for endothermic catalyticsteam plus hydrocarbon reforming reactions taking place in the GHR. Asan example using natural gas fuel, the PDX reactor has an exittemperature of about 1300° C. to about 1450° C. while an ATR reactorexit temperature is about 1000° C. to about 1100° C. The outlettemperature of the GHR reactor is between 550° C. and 650° C. Thesignificantly lower exit temperature results in the an increase in theproduction of hydrogen of between 35% and 40% for a PDX+GHR combinationcompared to a PDX reactor alone, both systems using the same quantity ofhydrocarbon feed and where the extra heat available from the PDX productgas stream is used not for hydrogen production but to produce steam forpower production in an associated power system. A further advantage ofthe two stage syngas production system is its ability to operate atsyngas delivery pressures up to 100 bar with less than 5% unconvertedmethane from the feed hydrocarbon fuel present in the product syngasstream. System components suitable for carrying out a two stage syngasproduction method are described in U.S. Pat. Nos. 9,327,972 and8,685,358, the disclosures of which are incorporated herein byreference. Hydrogen production should be maximized due to its muchhigher value compared to power production using excess steam.

The present disclosure further can provide for CO₂ capture inconventional H₂ systems, such as SMR. The state of art SMR system withCO₂ capture typically rely on the use of H₂-PSA waste gas as the fueland the use of an AGR-based CO₂ separation unit on the exhaust of theSMR furnace. Such a system typically captures up to 90% of overall CO₂from the process and produces H₂ that is about 45% more expensive thanH₂ without CCS.

In one or more embodiments, the present systems and methods can utilizethe unavoidable excess heat generated in the hydrogen plant (e.g., at atemperature level below 400° C.) to provide additional heat input toother systems and methods that optionally may be combined with thehydrogen production system. For example, the excess heat from thehydrogen production can be added to a power production system and methodto improve efficiency of such system and method. Hydrogen productionsystems commonly use a CO shift reactor to convert CO+H₂O to H₂+CO₂ withheat release so that in cooling the crude H₂ product stream to ambienttemperature prior to purification there is a very large heat release atrelatively low temperature level due to the sensible heat of the gasstream and the latent heat of condensation of the excess steam presentwhich can ideally be used as an added heat source to other systems. Suchadded heat can be beneficial, as one example, to assist in achievinghigh electrical generation efficiency in a power production system.

In other embodiments, the present disclosure encompasses the provisionof heat to the hydrogen production system. In particular, heat can beadded to the hydrogen production system (e.g., at a temperature level ofabout 400° C. to about 1000° C.) and can be useful specifically forsuperheating one or both of a fuel stream (e.g., natural gas) and asteam feed stream to an H₂+CO synthesis gas generation reactor system(e.g., any one or more of an SMR, a PDX, an ATR, a PDX+GHR, or anATR+GHR). The added heat that is input to the hydrogen production systemcan be provided from a variety of sources including, but not limited to,power production systems where high temperature combustion productstreams are available.

In further embodiments, the hydrogen production system can include asteam generating boiler that can be useful for cooling the product gasfrom the H₂+CO reactor system and producing high pressure saturatedsteam, which can be superheated using high temperature heat derived froma different source. The superheated steam together with preheatedhydrocarbon feed can then provide the feed to the H₂+CO reactor units.Any excess steam production can then be transferred to a further system.The H₂+CO syngas leaving the steam generating waste heat boiler (WHB)contains a substantial fraction of steam. It is then passed through acatalytic shift reactor where the steam combines with the CO in anendothermic reaction to produce H₂ and CO₂. The crude hydrogen streammust be cooled to near ambient temperature from a typical hightemperature level of about 400° C. The sensible heat rejected plus theadditional heat produced from the condensation of the residual steamcontent produces a considerable excess heat release available afterpreheating H₂ reactor boiler feed water and reactor feed streams to aclose temperature approach to the syngas stream leaving the steamgenerator. This excess heat can be transferred to a further system. Notethat optionally a second lower temperature catalytic shift reactor canbe used to maximize H₂ production. The present systems and methods canutilize a pressure swing adsorption (PSA) system to separate pure highpressure hydrogen from a cooled, crude hydrogen stream. The waste gasstream from the PSA unit at a pressure of about 1.2 bar to about 1.6 barcontains all the CO₂ produced from conversion of the hydrocarbon feed toH₂ together with CH₄+CO+H₂, and it is saturated with water vapor.

In additional embodiments, the present disclosure can provide for therecovery of substantially all the carbon present in the fuel for thehydrogen plant as CO₂, which can be compressed to pipeline pressure inthe range of about 100 bar to about 200 bar for disposal. For example,this can be achieved by treating the ambient temperature crude H₂ streamin an amine CO₂ scrubbing system upstream of the PSA. The waste gas fromthe PSA can then be used as a minor portion of a fuel stream consumed ina combined or separate system. The disadvantage of the amine CO₂ removalsystem is its high capital cost and the large quantity of low pressuresteam required for amine regeneration to produce the pure CO₂ productstream. The PSA waste gas stream contains a significant quantity ofH₂+CO. The waste gas can be compressed, and with added steam, passedthrough a catalytic CO shift reactor which results in the cooledcompressed waste gas stream having a H₂ molar concentration in the rangeof about 60% to about 85%. This stream can then be processed in a secondPSA unit giving an additional H₂ production. This combination of aminescrubbing plus first stage PSA plus CO shift plus second stage PSAresults in an overall ratio of H₂ product divided by (H₂+CO) present inthe syngas reactor product stream of greater than 95% and preferablygreater than 97%. The hydrogen production system can preferably beconfigured so that a monoethanolamine (MEA) unit or a physical solventCO₂ removal unit upstream of the first PSA is eliminated leaving all theCO₂ in the PSA waste gas stream.

Following compression and drying, this stream can be cooled to atemperature in the range of about 2° C. to about 10° C. above the CO₂freezing temperature at which point the separation of the liquid phaseand the vapor phase will result in greater than 70% and preferablygreater than 80% of the CO₂ being removed as a liquid. Optionally theliquid CO₂ can be treated in a stripping distillation column to removedissolved H₂+CO+CH₄ which will be transferred to the vapor phase. Theprocess is described in U.S. Pat. No. 7,819,951, which is incorporatedherein by reference. Other CO₂ removal systems including components thatmay be incorporated herein are disclosed in U.S. Pat. Nos. 8,021,464 and8,257,476, the disclosures of which are incorporated herein byreference. The separated vapor stream which is within 2 bar of the wastegas compressor discharge pressure is then warmed to atmospherictemperature, optionally passed through a CO shift catalytic reactorsystem with some added steam and treated as before in a second PSA unitwhich delivers H₂ at the same purity and pressure as the first PSA unit.A further preferred arrangement is to take the ambient temperature-gasstream separated from the bulk of the CO₂, in the low temperature CO₂removal system and recycle it back to the feed streams for the H₂+COsynthesis gas generation reactor. By closing the recycle loopcompletely, inert components can be vented from the system, and thisvented fuel gas stream can be consumed in a combined or separate system.The level of argon derived from the oxygen stream and nitrogen derivedfrom both the hydrocarbon feed and the oxygen streams must be kept at alow total concentration of from 3% to 12% (molar) in the feed gas to thefirst PSA. This arrangement does not require a second CO shift and PSAsystem. All the hydrogen will be produced from the main PSA while allthe CO₂ will be produced from the low temperature CO₂ removal system.

If desired, part or all of the oxygen used in the present systems andmethods can be supplied from a cryogenic air separation plant or from ahigh temperature oxygen ion transport membrane (ITM) unit which has alow-pressure air feed. The oxygen can be produced from the ITM unit as aproduct O₂ gas stream or it can immediately react with a fuel gas suchas natural gas mixed with a suitable diluent such as CO₂ in an ITMoxy-fuel combustor or diluted with steam to produce H₂+CO syngas in anITM reactor. The hydrogen plant can utilize a stream of high pressuregaseous oxygen at pressures up to 105 bar as feed to the H₂+CO synthesisgas generation reactor producing substantially pure H₂ at up to 95 barfrom the PSA system. A cryogenic air separation plant supplying highpressure oxygen can be particularly useful to provide the oxygen.

In one or more embodiments, the hydrogen production system and methodcan be combined with a power production system and method in order toimprove efficiency of both systems. For example, in some embodiments, apulverized coal fired power station generating high pressure superheatedsteam for turbines has available in the convection section flue gasleaving the super-heaters at temperatures in excess of 800° C. The feedstreams of hydrocarbon gas and steam for the syngas generation reactorscan be superheated to temperatures in the range 400° C. to 600° C. Thelow level excess heat available from the H₂ production system can beused to heat part of the power station boiler feed water releasing steamwhich would normally be used for extra power production in the steamturbines. CO₂ removal in the power station would need to use eitheramine scrubbing of the stack gas or the use of oxy-fuel coal combustionwith recycle of flue gas followed by CO₂ purification based onestablished technology.

As a further example, a gas turbine combined cycle power generationsystem uses a hydrocarbon fuel, usually natural gas, which is burned inthe gas turbine combustor. The fuel can be hydrogen which wouldgenerally be diluted with nitrogen or steam to reduce adiabatic flametemperature. The integration with the hydrogen production system isparticularly advantageous since it is possible not only for heatintegration to take place but also for the hydrogen production to besufficiently high to provide all the hydrogen fuel gas required by thegas turbine and also excess hydrogen for other uses. The integration notonly increases efficiency but also eliminates near 100% of the CO₂derived from combustion of the total hydrocarbon feed to the system.This is a very large improvement on the current system for CO₂ removalbased on amine scrubbing of CO₂ from the gas turbine outlet stream. Thesyngas reactor feed streams can be preheated against the gas turbineexhaust which for an industrial unit is in the temperature range ofabout 500° C. to about 620° C. The low temperature heat released fromthe hydrogen plant can be used for boiler feed-water preheatingreleasing stem for extra power production in the steam turbine.

In one or more embodiments, the present disclosure can provide ahydrogen production system that can be configured for integration with afurther system that is configured to provide added heat to the hydrogenproduction system. In particular, the system can comprise: a CO+H₂syngas reactor operating, for example, at up to 110 bar pressure withfeed streams of hydrocarbon fuel, steam, and optionally waste fuel gasplus CO₂, (preferably wherein the reactor system can comprise one ormore of an SMR, a PDX, an ATR, a PDX+GHR, or an ATR+GHR); a waste heatboiler configured to cool syngas produced in the reactor system andproduce saturated high pressure steam; a super-heater, which elevatesthe temperature of the reactor feed streams to a temperature in therange of about 400° C. to about 600° C.; one or more catalytic CO shiftreactors, which convert CO by reaction with contained steam to produceH₂+CO₂; a heat exchanger system configured to cool the syngas andcondense excess steam, which provides heat required for preheatingboiler feed water and optionally syngas reactor feed streams to atemperature of up to about 400° C.; a first pressure swing H₂purification unit (PSA) producing substantially pure H₂ product at apressure within about 5 bar of the syngas reactor outlet pressure and awaste gas steam at a pressure of about 1.2 bar to about 1.6 bar;optionally a chemical or physical absorbent CO₂ removal system placedupstream of the first PSA unit; a compressor to compress the PSA wastegas stream to a pressure of about 2 bar to about 5 bar higher than thefirst PSA H₂ product stream; optionally a catalytic CO shift reactorsystem using added steam to convert CO in the compressed waste gas byreaction with steam to H₂+CO₂; a second PSA, which processes the wastegas stream which contains more than 60% molar H₂ concentration toproduce a second substantially pure H₂ product stream at substantiallythe same pressure as the first H₂ product stream; and an outlet line foroutput of the waste fuel gas stream from the second PSA. In someembodiments, the system may include one or more lines for transfer ofexcess heat available from the syngas cooling duty and/or one or morelines for output of any excess steam or waste fuel gas from the H₂production system. Optionally, the CO₂ removal system upstream of thefirst PSA unit may be eliminated. Further, optionally, the use of a CO₂removal unit based on the principle of cooling the compressed and driedfirst PSA waste gas steam to within a temperature of 2° C. to 10° C. ofthe CO₂ freezing temperature and separating the liquid CO₂ from theresidual waste gas stream with provision for purifying the CO₂ may alsobe eliminated. Also, optionally, the waste gas from the first PSA unitfollowing waste gas compression and CO₂ removal can be recycled for useas part of the fuel gas feed to the syngas reactors. In order to preventa build-up of inert argon plus nitrogen in the closed cycle loopaccording to such embodiments, there will be a purge gas stream takenconveniently upstream of the first PSA to limit the concentration ofinerts to about 3% to about 12% (molar) concentration.

The integration of the hydrogen production system with a gas turbinecombined cycle power generation system will, in addition to heatintegration, use at least a portion of the produced hydrogen to provideall of the fuel gas required to power the gas turbine. The hydrogen willbe suitably diluted with nitrogen derived from the cryogenic O₂ plantproviding oxygen for the PDX+GHR or the ATR+GHR syngas reactors andalso, optionally, with excess heat and steam at a temperature levelbelow 400° C. derived from the hydrogen production system. This willresult in the near 100% recovery of CO₂ derived from combustion of thetotal hydrocarbon feed to the H₂ production plus the power productionsystems.

In one or more embodiments, the present disclosure provides a simple andeconomic process to capture and purify CO₂ as a by-product from wastestreams generated from various processes such as oxy-fuel combustion andpower generation, natural gas processing, and hydrogen generation. Thesystems and methods can be potentially utilized to purify and separateCO₂ from any industrial waste stream wherein an impure stream of CO₂with at least 40 mol % CO₂ content exist or where lower concentration ofCO₂ can be upgraded to at least 40 mol % concentration.

The presently discloses systems and methods can utilize knownrefrigeration methods to separate the contaminants in a process wastestream from CO₂. The present systems and methods, however, can utilize aunique arrangement of equipment that greatly simplifies the process andthus the cost of separation of purification of CO₂. The present systemsand methods are particularly useful when integrated with a hydrogenproduction plant in which the hydrocarbon feed is converted to H₂+CO ina pressurized system by reaction with oxygen and steam and in which theprocess integration between the H₂ production and CO₂ removal unitsachieves substantially 100% CO₂ capture.

In one or more embodiments, the present disclosure can be configured togenerate a purified and clean CO₂ stream from a CO₂ containing processwaste stream using refrigeration and fractionation. Briefly, the impureCO₂ stream is cooled down to a temperature near the CO₂ triple point(−56.4° C.) to liquefy the CO₂ content followed by separation andpurification in a mass transfer column. The process can be integratedwith a pressurized hydrogen production system with internal transferstreams to achieve efficient low cost 100% CO₂ capture.

In some embodiments, the present disclosure relates to a process forseparating CO₂ from contaminating components comprising methane, carbonmonoxide, hydrogen, nitrogen, argon, oxygen, and water vaporcharacterized by a mass transfer separation column system for processingan impure liquid carbon dioxide stream at a temperature close to thefreezing point of CO₂ to produce contaminant-enriched overhead vapor andcarbon dioxide-enriched bottoms liquid product stream.

The separation column can have a reboiler for boiling a portion of thecarbon dioxide-enriched bottoms liquid by indirect heat exchange againstcooling impure carbon dioxide fluid to produce cooled impure carbondioxide fluid for feeding and condensing said column system and warmedcarbon dioxide-enriched fluid.

The disclosed systems and methods can comprise a heat exchanger forfurther cooling impure carbon dioxide fluid by indirect heat exchange toproduce partially condensed impure carbon dioxide fluid.

The discloses systems and methods can comprise a first pressurereduction arrangement for reducing the pressure of impure liquid carbondioxide to produce reduced pressure impure liquid carbon dioxide whichis within 10° C. of the freezing point of the impure carbon dioxideliquid.

The discloses systems and methods can comprise further pressurereduction arrangements for expanding portions of the carbon dioxideenriched bottoms liquid to produce expanded carbon dioxide-enrichedbottoms liquid streams at reduced pressure to be used as refrigerantstreams to cool the impure carbon dioxide feed stream.

The impure carbon dioxide feed stream can be at least a portion of thewaste gas stream from a first H₂ PSA train placed upstream of the CO₂separation and purification step.

The pressure of the impure feed stream can be increased to give a CO₂partial pressure of at least 15 bar.

At least a portion of the overhead vapor from the mass transfer columnin the CO₂ separation system can be optionally compressed and recycledback to the H₂ plus CO syngas generation system of a pressurizedhydrogen plant.

Overhead vapor from the mass transfer column can be optionallycompressed and recycled back to a combined syngas generator equipment,comprised of a partial oxidation zone, a gas heated reformer zone, andwaste heat boiler heat recovery heat exchanger.

The compressed overhead vapor from the separation column can beprocessed in a second H₂ PSA unit recovering at least 60 mol % of the H₂in the separation column waste gas as a second H₂ product stream.

The CO₂ mass transfer column overhead vapor can be processed tocatalytically react contained carbon monoxide with steam to produceadditional hydrogen in a low temperature water-gas shift reactor toincrease its H₂ content to at least 60% on a mole basis prior to thesecond H₂ PSA train.

At least a portion of the waste gas from the second H₂ PSA unit can bemixed with the waste gas from the first H₂ PSA and recycled back to theCO₂ separation train.

At least a portion of CO₂ separation train waste gas can be used as afuel in a gas turbine, process heater, or an oxy-fuel burner.

At least a portion of the second H₂ PSA waste gas can be used as a fuelsource for any purpose including in a gas turbine, process heater, anoxy-fuel burner, or the furnace of a steam methane reforming reactor(SMR).

In all cases, the produced CO₂ can be compressed to pipeline pressurefor delivery to a suitable sequestration site.

In example embodiments, the present disclosure can provide a process forseparating carbon dioxide (CO₂) from a process stream comprising CO₂ andone or more further components. In particular, the process can comprise:providing the process stream at a pressure such that a partial pressureof the CO₂ in the process stream is at least 15 bar; drying the processstream sufficiently so that a dew point of the process stream comprisingthe CO₂ is reduced to a temperature of about −20° C. or less; coolingthe process stream in at least one heat exchanger to provide the processstream comprising the CO₂ as a two phase stream; expanding the two phasestream so as to reduce the temperature of the two phase stream to atemperature that is within about 15° C. of a freezing point of the twophase stream; and separating the two phase stream to provide a vaporstream enriched with at least one of the one or more further componentsand to provide a liquid stream that is enriched with the CO₂. In one ormore further embodiments, the process can be further characterized inrelation to one or more of the following statements, which may becombined in any number and order.

The drying can comprise passage of the process stream comprising the CO₂through a desiccant-packed bed.

The cooling can comprise cooling the process stream against at least aportion of the liquid stream that is enriched with the CO₂.

The cooling can comprise cooling the process stream in a first heatexchanger and in a second heat exchanger.

The cooling can comprise cooling the process stream in the first heatexchanger against a first portion of the liquid stream that is enrichedwith the CO₂ and cooling the process stream in the second heat exchangeragainst a second portion of the liquid stream that is enriched with theCO₂.

The process further can comprise expanding the first portion of theliquid stream that is enriched with the CO₂ and the second portion ofthe liquid stream that is enriched with the CO₂ so as to reduce thetemperature of the first portion of the liquid stream that is enrichedwith the CO₂ and the second portion of the liquid stream that isenriched with the CO₂ prior to cooling the process stream in the firstheat exchanger against the first portion of the liquid stream that isenriched with the CO₂ and cooling the process stream in the second heatexchanger against the second portion of the liquid stream that isenriched with the CO₂.

The first portion of the liquid stream that is enriched with the CO₂ andthe second portion of the liquid stream that is enriched with the CO₂can be separately expanded using separate valves.

The process further can comprise cooling the process stream in areboiler heat exchanger.

The process further can comprise passing at least a portion of theliquid stream that is enriched with the CO₂ through the reboiler heatexchanger.

The cooling can comprise cooling the process stream against at least aportion of the vapor stream enriched with at least one of the one ormore further components.

The process can comprise expanding the two phase stream so as to reducethe temperature of the two phase stream to a temperature that is withinabout 10° C. or about 5° C. of the freezing point of the two phasestream.

The separating the two phase stream can comprise passing the two phasestream through a distillation column.

The distillation column can include a stripping section below a feedpoint of the two phase stream into the distillation column and includesa rectifying section above the feed point of the two phase stream intothe distillation column.

The process can comprise separating the liquid stream that is enrichedwith the CO₂ into a first liquid CO₂ stream, a second liquid CO₂ stream,and a third liquid CO₂ stream.

The process can comprise independently expanding one, two, or three ofthe first liquid CO₂ stream, the second liquid CO₂ stream, and the thirdliquid CO₂ stream so as to reduce a temperature thereof and form arefrigerant stream.

The process can comprise compressing one, two, or three of the firstliquid CO₂ stream, the second liquid CO₂ stream, and the third liquidCO₂ stream.

The process can comprise compressing the vapor stream enriched with atleast one of the one or more further components.

The one or more further components can be one or more of a hydrocarbon,carbon monoxide, hydrogen, nitrogen, argon, and water vapor.

The process can comprise expanding the vapor stream enriched with atleast one of the one or more further components so as to reduce atemperature thereof and form a refrigerant stream.

The process can comprise passing at least a portion of the vapor streamenriched with at least one of the one or more further components througha pressure swing absorber unit.

The passing can be effective to recover at least 60 mol % or at least 75mol % of any H₂ present in the vapor stream enriched with at least oneof the one or more further components.

The process can comprise recycling at least a portion of the vaporstream enriched with at least one of the one or more further componentsfor combination with the process stream prior to said drying step. Forexample, at least a portion of the waste gas from the low temperatureCO₂ removal system and/or a second PSA can be recycled back to a GHR ina hydrogen production process. As another example, at least a portion ofthe waste gas from the low temperature CO₂ removal system and/or asecond PSA can be recycled back to a PDX reactor in a hydrogenproduction process. As still another example, at least a portion of thewaste gas from the low temperature CO₂ removal system and/or a secondPSA can be recycled back to a combined reactor in a hydrogen productionprocess. Such combined reactor can be a reactor unit that is a combinedpressure vessel comprised of a partial oxidation zone at the bottom, agas heated reformer zone with open-ended tubes in the middle, and awaste heat boiler heat exchanger at the top. In such configuration, asingle combined syngas stream and superheated steam can be main productsleaving the pressure vessel.

The process stream can be an H₂+CO₂ stream from a hydrogen productionprocess.

The process can be carried out without using an external refrigerant.

In example embodiments, the present disclosure particularly can providea carbon dioxide (CO₂) separation system. In particular, such system cancomprise: a compressor configured for compressing a process stream,wherein the process stream comprises CO₂ and one or more furthercomponents; a drier configured for removing moisture from the processstream; at least one heat exchanger configured for cooling the processstream against one or more cooling streams and providing the processstream as a two-phase stream; at least one expander configured forcooling the two-phase stream via expansion of the two-phase stream; anda mass transfer column configured to receive the two phase stream andgenerate a vapor phase stream and a liquid phase stream.

In example embodiments, the present disclosure can provide a hydrogenproduction system. In particular, such hydrogen production system cancomprise: a reactor unit configured for receiving a hydrocarbon feedstream and oxygen and forming a product gas stream comprising H₂+CO; asteam generating boiler configured for cooling the product gas streamcomprising H₂+CO and for forming steam; at least one reactor configuredfor receiving the product gas stream comprising H₂+CO and providing astream comprising H₂+CO₂; a pressure swing adsorber configured toreceive the stream comprising H₂+CO₂ and provide a product stream formedof substantially pure hydrogen and also provide waste gas steamcomprising CO₂; a compressor configured for compressing the waste gasstream comprising the CO₂; a drier configured for removing moisture fromthe waste gas stream comprising the CO₂; at least one heat exchangerconfigured for cooling the waste gas stream comprising the CO₂ againstone or more cooling streams and providing the waste gas streamcomprising the CO₂ as a two-phase stream; at least one expanderconfigured for cooling the two-phase stream via expansion of thetwo-phase stream; and a separator configured for separating thetwo-phase stream into a vapor phase stream and a liquid phase stream. Infurther embodiments, the hydrogen production system can be characterizedin relation to one or more of the following statements, which statementscan be combined in any number and order.

The hydrogen production system further can comprise one or more heatexchangers configured for heating the hydrocarbon feed stream againstone or both of the product gas stream comprising H₂+CO and the streamcomprising H₂+CO₂.

The hydrogen production system further can comprise one or more heatexchangers configured for transfer of excess heat to an externalprocess.

The hydrogen production system further can comprise one or more linesconfigured for output of one or both of a waste fuel gas stream andsteam generated in the hydrogen production system.

The hydrogen production system further can comprise one or more linesconfigured for delivery of at least part of the product stream formed ofsubstantially pure hydrogen as fuel to a gas turbine.

The reactor unit can comprise a steam plus hydrocarbon plus optionallyCO₂ catalytic reformer.

The reactor unit can comprise a partial oxidation unit.

The reactor unit can comprise a catalytic auto-thermal reformer.

The reactor unit can comprise a first stage unit that is either anauto-thermal reformer or a partial oxidation reactor and comprises asecond stage gas heated steam plus hydrocarbon catalytic reformer.

At least part of the H₂+CO stream produced from the reactor unit can begenerated in an ITM partial oxidation reactor using a low pressurepreheated feed air stream air stream.

The hydrogen production system of further can comprise a super-heaterheat exchanger configured to transfer heat from an external heat sourceto at least the hydrocarbon feed stream.

The reactor unit can be a combined pressure vessel comprised of apartial oxidation zone and a gas heated reformer.

The partial oxidation zone can be at a bottom portion of the combinedpressure vessel, and the gas heated reformer can comprise open-endedtubes in a middle zone of the combined pressure vessel and a waste heatboiler heat exchanger at a top portion of the combined pressure vessel.

In example embodiments, the present disclosure can provide a process forhydrogen production. In particular, the process can comprise: reacting ahydrocarbon feed stream and oxygen into a reactor unit to form a productgas stream comprising H₂+CO; passing the product gas stream comprisingH₂+CO through a steam generating boiler to add steam to the product gasstream comprising H₂+CO; converting the product gas stream comprisingH₂+CO in at least one reactor to form a stream comprising H₂+CO₂;processing the stream comprising H₂+CO₂ in a pressure swing adsorber toprovide a product stream formed of substantially pure hydrogen and alsoprovide waste gas steam comprising CO₂; forming a liquid CO₂ productstream in a cryogenic separation unit operating with auto-refrigerationby passing the waste gas stream comprising CO₂ therethrough such that atleast 50 mol % of the CO₂ in the waste gas stream comprising CO₂ isseparated into the liquid CO₂ product stream; and recycling a vaporphase stream from the cryogenic separation unit. In further embodiments,the process can be characterized in relation to one or more of thefollowing statements, which can be combined in any number and order.

The cryogenic separation unit operating with auto-refrigeration canoperate without using an external refrigerant.

The cryogenic separation unit can comprise: a drier configured forremoving moisture from the waste gas stream comprising CO₂; at least oneheat exchanger configured for cooling the waste gas stream comprisingCO₂ against one or more cooling streams and providing the waste gasstream comprising CO₂ as a two-phase stream; and at least one expanderconfigured for cooling the two-phase stream via expansion of thetwo-phase stream.

The cryogenic separation unit further can comprise: a compressorconfigured for compressing the waste gas stream comprising CO₂, thecompressor being positioned upstream from the drier; and a separatorconfigured for separating the two-phase stream into the vapor phasestream and the liquid CO₂ product stream.

The process can comprise removing CO₂ from the stream comprising H₂+CO₂prior to processing the stream comprising H₂+CO₂ in the pressure swingadsorber.

The removing of CO₂ from the stream comprising H₂+CO₂ can comprisepassing the removing CO₂ from the stream comprising H₂+CO₂ through achemical or physical solvent based CO₂ removal unit.

A portion of the waste gas steam comprising CO₂ exiting the pressureswing adsorber can be compressed and recycled back to the reactor unit.

At least a portion of the vapor phase stream from the cryogenicseparation unit can be recycled back to the reactor unit.

The vapor phase stream from the cryogenic separation unit can beprocessed through a second pressure swing absorber to remove at least aportion of any H₂ present in the vapor phase stream prior to recyclingof the vapor phase stream from the cryogenic separation unit.

The process can comprise removing at least a portion of any argon andnitrogen present in one or both of the product gas stream comprisingH₂+CO and the stream comprising H₂+CO₂ prior to entry of the streamcomprising H₂+CO₂ into the pressure swing absorber such that the totalconcentration of argon and nitrogen in the stream comprising H₂+CO₂ atan inlet of the pressure swing adsorber in the range of about 3 mol % toabout 12 mol %.

At least 80 mol % of the CO₂ in the waste gas stream comprising CO₂ canbe separated into the liquid CO₂ product stream.

The forming of the liquid CO₂ product stream in the cryogenic separationunit can comprise: providing the waste gas stream comprising CO₂ at apressure such that a partial pressure of the CO₂ in the process streamis at least 15 bar; drying the waste gas stream comprising CO₂sufficiently so that a dew point of the waste gas stream comprising CO₂is reduced to a temperature of about −20° C. or less; cooling the wastegas stream comprising CO₂ in at least one heat exchanger to provide thewaste gas stream comprising CO₂ as a two phase stream; expanding the twophase stream so as to reduce the temperature of the two phase stream toa temperature that is within about 15° C. of a freezing point of the twophase stream; and separating the two phase stream to provide the vaporphase stream and to provide the liquid CO₂ product stream.

The vapor phase stream from the cryogenic separation unit can be passedthrough a catalytic CO shift unit with an economizer heat exchanger, hassteam added thereto, and is then passed through a catalytic reactor toconvert at least a portion of the contained CO by reaction with thesteam to form a further stream comprising H₂+CO₂ and to form a gasstream containing at least 60 mol % H₂.

BRIEF DESCRIPTION OF THE DRAWINGS

Having thus described the disclosure in the foregoing general terms,reference will now be made to the accompanying drawings, which are notnecessarily drawn to scale, and wherein:

FIG. 1 is a flow diagram of a low temperature separation unit accordingto embodiments of the present disclosure useful for separation of carbondioxide from a process stream utilizing auto-refrigeration.

FIG. 2 is a flow diagram of a hydrogen production facility including alow temperature carbon dioxide separation unit according to embodimentsof the present disclosure.

DETAILED DESCRIPTION

The present subject matter will now be described more fully hereinafterwith reference to exemplary embodiments thereof. These exemplaryembodiments are described so that this disclosure will be thorough andcomplete, and will fully convey the scope of the subject matter to thoseskilled in the art. Indeed, the subject matter can be embodied in manydifferent forms and should not be construed as limited to theembodiments set forth herein; rather, these embodiments are provided sothat this disclosure will satisfy applicable legal requirements. As usedin the specification, and in the appended claims, the singular forms“a”, “an”, “the”, include plural referents unless the context clearlydictates otherwise.

The present disclosure provides systems and methods for production ofvarious materials that are typically gaseous at standard temperature andpressure (e.g., about 20° C. and about 1 bar). The systems and methodsare particularly suitable for production of hydrogen and/or carbondioxide. In one or more embodiments, the systems and methods can relateto the production of hydrogen alone or in combination with carbondioxide. Likewise, the systems and methods can relate to the productionof carbon dioxide that is separated from a process stream, and suchseparation can also relate to production of hydrogen. In someembodiments, the present systems and methods relate to processes usefulin separating carbon dioxide from a process stream that may or may notinclude hydrogen. In specific embodiments, the systems and methodsrelate to the production of hydrogen and production of carbon dioxideand can include producing a stream comprising both of hydrogen andcarbon dioxide and separating the carbon dioxide from the hydrogen toprovide a substantially pure stream of hydrogen and a substantially purestream of carbon dioxide.

In one or more embodiments, the present disclosure relates to systemsand methods suitable for separation of carbon dioxide from a processstream. The process stream may be any industrial process streamcomprising carbon dioxide. In some embodiments, the process stream maybe a stream from a hydrogen production process. In other embodiments,the process stream may be any further industrial process streamcomprising carbon dioxide wherein it can be beneficial to separate atleast a portion of the carbon dioxide therefrom. For example, referringto FIG. 2, the process stream may be any of streams 308, 331, and 309.As such, the carbon dioxide separation process may be combined with ahydrogen production process as described herein, or the carbon dioxideseparation process may be utilized with a different process stream.

A simplified block flow diagram of a carbon dioxide separation processaccording to the present disclosure is shown in FIG. 1. A seen therein,a process stream 101 containing CO₂ is provided. As noted above, theprocess stream 101 may be received from any source, such as a hydrogenproduction process. The process stream 101 can be compressed to apressure of at least 30 bar, at least 35 bar, or at least 40 bar (e.g.,to a maximum of 100 bar) within a compressor 200. In exampleembodiments, the compressor 200 may be an intercooled multi-stagecompressor. The compression step preferably will raise the partialpressure of the CO₂ within the waste stream to at least about 15 bar(e.g., up to a maximum, in some embodiments, of about 55 bar). The CO₂partial pressure can be raised to be in the range of about 15 bar toabout 55 bar, about 15 bar to about 45 bar, or about 15 bar to about 40bar. The compressed process stream 102 is then directed to a drier 205to reduce the moisture content of the compressed process stream and forma first impure CO₂ stream 103. The extent of moisture removal can beadjusted as desired such that the dew point of the process stream willbe reduced to a temperature as low as about −60° C. In variousembodiments, the dew point can be reduced to a temperature of about −10°C. or less, about −20° C. or less, or about −40° C. or less, such as toa low temperature of about −60° C. For example, the dew point can bereduced to a temperature in the range of about −60° C. to about −10° C.,about −60° C. to about −20° C., or about −60° C. to about −30° C. Thedrier 205, in some example embodiments, can be a drying bed packed withappropriate desiccant material, such as molecular sieves or zeolites.

The first impure CO₂ stream 103 is cooled to significantly reduce thetemperature thereof and ultimately form a two phase stream that is thensubject to rapid cooling utilizing auto-refrigeration. In someembodiments, auto-refrigeration can generally indicate that therefrigeration is carried out in the express absence of any externalrefrigerant. In other words, the streams are not cooled against atypical refrigerant stream, such as Freon, liquid nitrogen, liquidpropane, ammonia, or the like. Rather, the stream is only cooled againstfurther streams produced in the CO₂ separation process and usingexpansion techniques. In particular, auto-refrigeration can indicatethat at least one stream comprising a liquid component is expanded toprovide for rapid cooling of the stream.

Returning to FIG. 1, the first impure CO₂ stream 103 is directed to afirst heat exchanger 210 to partially cool down and form the secondimpure CO₂ stream 104. Thereafter, the second impure CO₂ stream 104 isdirected to a reboiler heat exchanger 215 to further cool down and formthe third impure CO₂ stream 105. The third impure CO₂ stream 105 isfurther cooled down in a second heat exchanger 211 to form a fourthimpure CO₂ stream 106. The foregoing cooling steps can be effective toprovide the impure CO₂ stream(s) in the form of a two phase streamincluding a gaseous component and a liquid component. In someembodiments, the two phase stream is at least partially formed duringpassage through the reboiler heat exchanger 215 and/or is formed duringpassage through the second heat exchanger 211.

To further facilitate cooling of the impure CO₂ stream, the fourthimpure CO₂ stream 106 is expanded within a first valve 220 to anappropriate pressure that would drop the temperature of the expandedimpure CO₂ stream 107 to near the CO₂ triple point temperature (−56.4°C.). For example, expansion of the stream 106 can be effective to reducethe temperature of the stream to within about 15° C., within about 10°C., or within about 5° C. of the freezing point of the CO₂ in thestream. A cold, two phase CO₂ stream 107 thus exits the first valve 220.

The cold two phase CO₂ stream 107 becomes a feed stream to the masstransfer column 225. The mass transfer column 225 has a strippingsection 226 below the feed point of stream 107 producing a high purityliquid CO₂ stream 108 as a bottom product and a rectifying section 227above the feed point of stream 107 producing a purified top vapor phaseproduct 109. The mass transfer column 225 is packed with appropriatepacking material to enhance the mass transfer within the column andcollection of the liquid CO₂ at high purity. The design of the strippingcolumn will be done such that it can effectively handle the two-phasefeed stream which could be done in variety of ways such as but notlimited to flashing the feed in a flash vessel prior to the entrance tothe stripping column, the use of a gallery tray or chimney tray withinthe column or any combination of thereof. The bottom liquid CO₂ product108 typically contains about 80 mol % and preferably at least 85 mol %of the total CO₂ within the impure CO₂ stream 107 while the rest of theCO₂ content and other volatile impurities within the feed waste streamwould end up in the overhead vapor phase stream 109. In variousembodiments, the bottom liquid CO₂ product 108 can contain at least 50mol %, at least 60 mol %, at least 70 mol %, or at least 80 mol % (e.g.,about 50 mol % to about 99 mol %, about 60 mol % to about 98 mol %,about 70 mol % to about 95 mol %, or about 75 mol % to about 90 mol %)of the total CO₂ within the cold two phase CO₂ stream 107. The bottomliquid CO₂ product 108 passes through the reboiler heat exchanger forfurther cooling and exits as purified a CO₂ product stream that splitsinto a first portion 110 and a second portion 150, which is recycledback into the bottom section of the mass transfer column 225.

The cool overhead vapor phase stream 109 can be used as a source ofrefrigeration to cool down the impure CO₂ streams in heat exchangers 210and 211. These two heat exchangers are preferably plate and fin typemade from aluminum and although they are shown as discrete blocks inFIG. 1, they may be designed and fabricated as a single unit with two(or more) sub-unit or sections. The system is suitably insulated. Theliquid CO₂ product 108 preferably is at least 80% molar pure CO₂, atleast 85% molar pure CO₂, at least 90% molar pure CO₂, at least 95%molar pure CO₂, at least 98% molar pure CO₂, at least 99% molar pureCO₂, at least 99.5% molar pure CO₂, or at least 99% molar pure CO₂.

To generate additional refrigeration duty, the purified CO₂ productstream portion 110 exiting the reboiler heat exchanger 215 can bedivided into 3 separate streams 111, 114, and 117. Purified CO₂ productstreams 111 and 114 can be reduced in pressure by expansion in valves230 and 235, respectively, to achieve appropriate temperature profilesin heat exchangers 210 and 211. Specifically, purified CO₂ productstream 111 exits valve 230 as stream 112 and passes through heatexchanger 211 to provide purified CO₂ stream 113. Similarly, purifiedCO₂ product stream 114 exits valve 235 as stream 115 and passes throughheat exchanger 210 to provide purified CO₂ stream 116. Although each ofstreams 112 and 115 are illustrated as passing through only one of heatexchangers 210 and 211, it is understood that one or both of streams 112and 115 may be passed through both of heat exchangers 210 and 211 priorto passing to the compression step described next. The purified CO₂streams (113, 116 and 117) will be partially pressurized and mixedwithin a compressor 240 to form a high density CO₂ stream 118 beforebeing raised in pressure to the required end-use pressure in a liquidpump 245 to leave as final CO₂ product stream 119. The final warmoverhead vapor phase stream 109 can be optionally compressed based onthe downstream application requirement.

An important feature of this arrangement is the capability of recyclingthe vapor phase stream 109 from the separation column 225 after warmingin heat exchanger 211 to form stream 120 and heating in heat exchanger210 to form stream 121 at near ambient temperature. The stream 121 canbe compressed in compressor 250 to form stream 122. The stream 122 canbe at least partially combined with original feed stream 101, and thisrecycle allows for a favorable increase in the overall CO₂ recovery fromthe process feed stream 101. Furthermore, the stream 122 can bepartially or completely recycled back as the feedstock to a chemicalproduction process (such as a hydrogen production process furtherdescribed below) and achieve up to 100% CO₂ capture from the chemicalproduction process.

In example embodiments, the presently disclosed systems and methods forcarbon dioxide separation particularly can be useful with hydrogengeneration processes or revamping of existing hydrogen generationprocesses that utilize only one H₂ separation train such as PSA beds ormembrane separators to achieve 100% CO₂ capture. Current methods ofthermochemical hydrogen generation typically rely on recovery ofhydrogen using PSA beds. Specifically, natural gas and steam (andoptionally oxygen) can be input to an H₂+CO syngas generation area alongwith a PSA waste gas. The product therefrom is subjected to syngascooling and shifting of the CO to H₂. Thereafter, PSA separation iscarried out to provide an H₂ product and the PSA waste gas. The PSAsrecover 75% to 90% of the total hydrogen in the feed gas. The PSA wastegas containing typically 10% to 15% of the hydrogen production togetherwith all the CO₂ produced from H₂ generation is generally burned withCO₂ vented to the atmosphere.

The systems and methods of the present disclosure can be utilized tocapture substantially 100% of the CO₂ from hydrogen generating processesby recovering CO₂ from a pressure swing absorber (PSA) waste stream.This can encompass, for example, utilizing a CO₂ separation process asdescribed above in combination with a hydrogen production process aswill be described below. Separation of CO₂ from PSA off-gas increasesthe hydrogen concentration in CO₂ separation train waste gas to at leastabout 60 mol % which would make it suitable and economic for additionalH₂ recovery within a second PSA. In addition, based on the concentrationof CO within CO₂ separation train waste gas, it can be optionallyshifted, prior to the second H₂ recovery step, using a small lowtemperature shift reactor to further increase its hydrogen content. Theoff-gas from the second PSA unit will be recycled back to the syngasgeneration reactors. It can also be optionally mixed with the off-gasfrom the first PSA to increase CO₂ recovery in the CO₂ cryogenicseparation system.

Previous efforts have been undertaken to provide for production ofhydrogen through combination with additional systems, and one or moreelements from such previous endeavors may be integrated into thepresently disclosed systems and methods. For example, U.S. Pat. No.6,534,551, the disclosure of which is incorporated herein by reference,describes the combination of: 1) a hydrocarbon fuel gas reaction withsteam and or oxygen; and 2) a power system utilizing a compressedoxidant gas in which a fuel gas is burned with combustor productsproducing power by work expansion and in which the expanded combustionproduct gas is used to superheat the steam used in hydrogen synthesisreactions and in which the oxygen production unit is driven by at leasta portion of the power produced by the expansion of the combustionproduct gas.

In one or more embodiments, the present systems and methods canbeneficially provide for hydrogen production with capture ofsubstantially all of the carbon produced, particularly substantially allof the CO₂ produced. In this manner, the present disclosure may refer toa hydrogen plant, and it is understood that such hydrogen plant refersto the combination of elements necessary to form the hydrogen productionsystem utilized herein. A hydrogen plant as described herein thus can beconfigured for producing substantially pure hydrogen and likewiseproducing substantially pure carbon dioxide that is separated from acrude hydrogen stream.

A hydrogen production plant for use according to the present disclosurecan incorporate any variety of elements known to be suitable in priorhydrogen production plants. In particular, the hydrogen production plantcan comprise a reactor unit configured for forming a stream comprisingCO+H₂ gas. The reactor unit can encompass a single element or aplurality of elements. For example, a reactor unit in a hydrogenproduction plant can comprise a two stage reactor unit including a firststage reactor which converts a hydrocarbon feed to a CO+H₂ gas. Suchso-called H₂+CO synthesis gas generation reactor can be any one or moreof a steam methane reforming (SMR) reactor, a partial oxidation (PDX)reactor, an autothermal reforming (ATR) reactor, a PDX+GHR (gas heatedreactor), or an ATR+GHR. In some embodiments, partial oxidation of anatural gas feed with pure oxygen can be carried out at an outlettemperature of about 1300° C. to about 1500° C. at typical pressures ofabout 30 bar to about 150 bar. An auto-thermal reformer can add steamand excess hydrocarbon, generally natural gas, after the partialoxidation burner so that the high temperature gases can then passthrough a bed of catalyst where subsequent steam-hydrocarbon reformingreactions take place yielding further H₂+CO and cooling the gas mixtureto an outlet temperature of about 1000° C. to about 1100° C. atpressures of about 30 bar to about 150 bar. The second stage reactor cancomprise a steam/hydrocarbon catalytic reformer in which the total H₂+COgas product from both reactors (e.g., at a temperature of about 1000° C.or greater) is used to provide the endothermic heat of the reformingreactions in a convectively heated shell side flow with catalyst in thetubes. Optionally the two reactors can operate in a series or parallelmode. A favorable configuration uses a vertical gas heated reformer(GHR) with catalyst filled open ended tubes hanging from a single tubesheet at the top of the vessel, with the product H₂+CO leaving thereformer tubes and mixing with the product gas from a PDX reactor or anATR in the base of the GHR, and the total product H₂+CO stream passingthrough the shell side and cooling typically from about 1050° C. to 550°C. to 800° C.

An advantage of the two reactor configuration is that the yield of H₂+COfrom hydrocarbon feed is maximized, and all CO₂ formed in the reactionsis contained within the high-pressure system. The product CO+H₂ gas isfurther cooled in a steam generating waste heat boiler (WHB), and afurther advantage is that this steam quantity is only sufficient toprovide the required steam flow to the two H₂+CO reactors with only asmall excess flow. The system has no large by-product steam production.

To generate hydrogen, the H₂+CO product leaving the WHB at a typicaltemperature of about 240° C. to about 290° C. and containing typicallyabout 20 mol % to about 40 mol % steam is passed through either one ortwo (or more) catalytic shift converters where CO reacts with steam toproduce CO₂ and more H₂. The reactions for the whole H₂ productionprocess sequence are shown below (using CH₄ as the hydrocarbon).

CH₄ + ½O₂ → CO + 2H₂  Partial oxidation CH₄ + 2O₂ → CO₂ + 2H₂O Combustion CH₄ + H₂O → CO + 3H₂  Steam reforming CH₄ + CO₂ → 2CO + 2H₂  Dry reforming CO + H₂O → CO₂ + H₂    CO shift

The total CO+H₂ product passing through the CO shift reactors is cooled,and a significant amount of heat is released generally at a temperaturelevel of up to 400° C. or lower as the gas cools and steam condenses.This heat is released not at a single temperature level but over atemperature range down to near ambient temperature. Part of this heatrelease can be used to preheat boiler feed water, to produce the steamrequired for syngas production in the reactors but there is a largeexcess quantity that is at a low temperature level and only availableover a temperature range.

The efficiency of the H₂+CO generation in the two reactors can besignificantly increased by preheating the hydrocarbon and steam feeds totypically about 400° C. to about 600° C. and preferably to about 500° C.to about 550° C. This preferably is done using an external heat sourcesince no excess heat at these temperature levels is available within theH₂+CO generation reactors plus WHB.

In one or more embodiments, systems and methods of producing the H₂+COsyngas which can be used to produce the pure hydrogen product streamaccording to the present disclosure may exhibit desired characteristicsthat can be beneficial for integration of the hydrogen production withother systems, such as power generation systems. The excess heatavailable over a temperature range from near ambient up to about 400° C.is ideal for boiler feed water heating in a steam based power cycle orfor heating a high pressure CO₂ stream. In each case the result is areduction in parasitic power demand and an increase in power cycleefficiency. The required external heat need to preheat the syngasreactor feed streams up to about 550° C. can easily be provided usinghigh temperature boiler flue gas leaving the super-heater in apulverized coal fired power boiler or using the hot turbine exhaust froman industrial gas turbine in a combined cycle power generation system orusing a further high temperature exhaust stream from a power productionsystem. The heat integration leads to an overall increase in theefficiency of a combined system.

The cooled H₂ rich gas stream is now passed through an ambient coolerwhere condensed water is removed. The gas stream is then passed througha conventional multi-bed pressure swing adsorber (PSA) which separatestypically about 85% to about 90% of the hydrogen as a pure stream havingtypically about 10 ppm to about 50 ppm total impurities. All theimpurities in the crude H₂ feed stream are separated as a waste fuel gasstream, which waste stream can comprise any combination of components,such as H₂, CO, CO₂, CH₄, N₂, Ar, and a small quantity of vapor phaseH₂O. The pressure is typically about 1.1 bar to about 1.6 bar. Thiswaste gas typically has about 20% of the total hydrocarbon reactorhydrocarbon feed lower heating value (LHV) so its efficient use iscritical to the overall economics of H₂ production. The waste gascontains all the carbon from the total hydrocarbon feed as CO₂+CO andthe recovery of this carbon as pure CO₂ at pipeline high pressure isvital to meet climate change emission objectives. In order to recoverthe carbon present in the hydrocarbon feed to the hydrogen plant as CO₂product the ideal objective is to convert residual CO by catalytic shiftreaction with added steam to produce CO₂+H₂ then separate the CO₂ as apure product stream. Three options are available which address thisproblem of CO₂ removal and the maximization of CO₂ recovery.

In some embodiments, CO₂ removal and the maximization of CO₂ recoverycan comprise adding a chemical or physical solvent scrubbing unit toremove all the CO₂ from the ambient temperature PSA feed stream. Forexample, this can be achieved by treating the ambient temperature crudeH₂ stream in an amine CO₂ scrubbing system upstream of the PSA. Thewaste gas from the PSA can then be used as a minor portion of the fuelstream consumed in the power system. The PSA waste gas stream contains asignificant quantity of H₂+CO. Alternatively, the waste gas stream canbe compressed to a pressure of 1 to 2 bar higher than the H₂ deliverypressure from the PSA and then passing this gas stream with added steamthrough a catalytic CO shift conversion unit which would convert over90% of the CO by reaction with steam to CO₂+H₂. The cooled product gasstream will now have a hydrogen concentration of 60% to 70% (molar).This gas stream can then be passed through a second multi-bed pressureswing adsorption unit to recover an additional H₂ product stream at thesame pressure and purity as the hydrogen from the first PSA. The wastegas from the second PSA unit which contains all the inert argon andnitrogen derived from the hydrocarbon and oxygen reactor feed streamscan beneficially be sent to the power plant for combustion. Thedisadvantage of the amine CO₂ removal system is its high capital costand the large quantity of low pressure steam required for amineregeneration to produce the pure CO₂ product stream. This combination ofamine scrubbing plus first stage PSA plus CO shift plus second stage PSAresults in an overall ratio of H₂ product divided by (H₂+CO) present inthe syngas reactor product stream of greater than 95% and preferablygreater than 97%.

In other embodiments, CO₂ removal and the maximization of CO₂ recoverycan comprise eliminating the MEA unit or the physical solvent CO₂removal unit upstream of the first PSA leaving all the CO₂ in the PSAwaste gas stream. The stream then can be treated utilizing cryogeniccooling for separation of the CO₂ as otherwise described herein.

In further embodiments, CO₂ removal and the maximization of CO₂ recoverycan comprise recycling one or more streams back to the feed streams forthe PDX or ATR or GHR or SMR reactors. By closing the recycle loopcompletely, inert components can be vented from the system. The ventedpurge gas stream can be taken at ambient temperature upstream of thefirst PSA and sent, for example, to a power plant for combustion. Thelevel of argon present in the oxygen stream and nitrogen present in boththe hydrocarbon feed and the oxygen streams are preferably kept at a lowtotal concentration of from about 3 mol % to about 12 mol % in the feedgas to the first PSA. This arrangement does not require a second COshift and PSA system. All the hydrogen will be produced from the mainPSA while all the CO₂ will be produced from the low temperature CO₂removal system. As further described herein, CO₂ separation can beapplied independent of the hydrogen production processes describedherein. Suitable CO₂ separations systems and methods are thus describedherein that may be applied to any process stream comprising CO₂.

Example embodiments of a hydrogen production plant (and an associatedhydrogen production process) are evident in relation to FIG. 2. Thehydrogen plant can be fueled with a hydrocarbon fuel source, preferablya gaseous hydrocarbon, and more preferably with substantially puremethane. The example embodiment of FIG. 2 is described in relation tothe use of methane as the hydrocarbon. In FIG. 2, the methane in stream300 is compressed in compressor 401 to a pressure of about 20 bar toabout 120 bar, about 40 bar to about 110 bar, or about 60 bar to about100 bar. The compressed methane stream is passed through a heatexchanger 412 to heat the methane stream to a temperature of about 300°C. to about 700° C., about 350° C. to about 650° C., or about 400° C. toabout 600° C. The methane exiting the heat exchanger 412 is split intotwo streams 302 and 303. The methane is thus directed to a reactor unitthat, as exemplified in FIG. 2, is formed of a PDX reactor 402 and a GHR403. In other embodiments, it is understood that the reactor unit may beformed of a single device or multiple devices as otherwise alreadydiscussed herein. The methane in stream 302 combined in the PDX reactorwith an oxygen stream 301 that is pre-heated in heater 418 prior topassage into the PDX reactor. Preferably, the oxygen stream 301 can beabout 99.5% pure O₂ and can be taken, for example, from a cryogenic airseparation plant (not illustrated). The oxygen entering the PDX reactor302 may be at a pressure in the range of about 20 bar to about 120 bar,about 40 bar to about 110 bar, or about 60 bar to about 100 bar.

The methane is partially oxidized in the PDX reactor 302 with the oxygento produce a product H₂+CO stream 330 at a temperature of about 700° C.to about 1800° C., about 900° C. to about 1700° C., or about 1100° C. toabout 1600° C. The product H₂+CO stream 330 optionally be quenched andcooled by the addition of a quenching stream, such as to a temperaturethat is about 50° C. or more, about 75° C. or more, or about 100° C. ormore below the temperature of the product H₂+CO stream 330 directlyexiting the PDX reactor 402. The optionally quenched product H₂+COstream 330 enters the base of the GHR reactor 403, undergoes endothermicreforming reactions, and leaves the GHR as stream 304. The total productCO+H₂ stream can exit the GHR 304 at a temperature of about 300° C. toabout 900° C., about 400° C. to about 800° C., or about 500° C. to about700° C. The total product CO+H₂ stream 304 passes through the waste heatboiler 404 and exits in stream 305 at a temperature in a range of about150° C. to about 450° C., about 200° C. to about 425° C., or about 250°C. to about 400° C. The waste heat boiler can be a steam generatingboiler and thus can be effective to add steam to the total product CO+H₂stream.

The product stream comprising H₂+CO is then reacted in at least onereactor to form a stream comprising H₂+CO₂. As illustrated in FIG. 2,the total product CO+H₂ stream 305 passes through a first catalystfilled CO shift reactor 405 and a second catalyst filled CO shiftreactor 406 in series with respective outlet streams 306 and 308. Theoutlet stream 308 passes through heat recovery heat exchanger 420, andthe outlet stream 308 passes through heat recovery heat exchanger 414and, in each of the heat exchangers, heat is used to heat boilerfeed-water preheating streams to provide boiler feed-water for wasteheat boiler 404.

The stream 308 comprises H₂+CO₂, but it is understood that any streamdescribed herein as comprising H₂+CO₂ only defines the minimalcomposition of the stream, and further materials may be present in saidstream, such as carbon monoxide and one or more carbon-containingmaterials. After stream 308 passes through the heat exchanger 414, thestream 308 is cooled in water cooler 416 to near ambient temperature andexits as cooled, crude H₂+CO₂ stream 331. The crude H₂+CO₂ stream 331preferably can contain substantially all of the CO₂ derived fromcombustion of carbon in the hydrocarbon feed together with water vaporand minor amounts of CO, CH₄, N₂ and Ar. Condensed water is separatedfrom cooled, crude H₂+CO₂ stream 331 in separator 407. Water stream 332from the separator 407 and cooled boiler feed-water stream 334 enter awater treatment unit 411 which produces purified water 55 and an excesswater stream 61. The purified water stream 335 (which is recycled foruse as the boiler feed-water) is pumped to about 87 bar pressure in pump415, and boiler feed water stream 316 enters the heat exchanger 414before passing through heat exchanger 420 to the waste heat boiler 404.The boiler feed-water exiting pump 13 can be at a pressure in the rangeof about 50 bar to about 120 bar, about 60 bar to about 110 bar, orabout 70 bar to about 100 bar.

The saturated steam stream 317 leaving the waste heat boiler 404 firstpasses through heat exchanger 412 to exit as stream 318, which iscompressed in compressor 413. Stream 329 exiting the compressor 413branches, and steam stream 319 passes through the heat exchanger 412before combining with methane stream 303 for entry into the GHR 403.Steam in stream 333 passes back through heat exchanger 414 to exit asstream 334 for passage into the water tank/water treatment unit 411.

The steam stream 319 fed to the GHR reactor 403 provides a steam tocarbon ratio (carbon combined with hydrogen in the GHR reactor feed) of6:1 in this case. This high ratio allows 80 bar H₂+CO productionpressure with a low quantity of unconverted methane in the total productH₂+CO stream 304. In some embodiments, the steam to carbon ratio can beabout 2:1 to about 10:1, about 3:1 to about 9:1, or about 4:1 to about8:1. Preferably, the steam to carbon ratio is at least 3:1, at least4:1, or at least 5:1.

The purified H₂+CO₂ product in stream 309 exits the separator 401 and isnext processed in a pressure swing adsorber 408 to provide a productstream formed of substantially pure hydrogen in stream 310 and alsoprovide waste gas comprising CO₂ in stream 311. For example, thesubstantially pure H₂ product stream 310 can be at a pressure of about50 bar to about 120 bar, about 60 bar to about 110 bar, or about 65 barto about 100 bar and can have an impurity level of about 10 ppm to about200 ppm impurity, about 20 ppm to about 175 ppm impurity, or about 25ppm to about 150 ppm impurity. In some embodiments, the substantiallypure H₂ product stream 310 can comprise about 60% to about 98%, about70% to about 95%, or about 75% to about 92% of the hydrogen from stream309.

The waste gas in stream 311 preferably contains all the CO₂ plus CO, H₂,CH₄, Argon, N₂ and traces of water vapor previously in stream 309. Thewaste gas stream 311 is then processed in a low temperature separationunit 409 (e.g., a cryogenic separation unit) as otherwise describedherein to form a liquid CO₂ product stream. As discussed above, this ispreferably carried out such that at least 50 mol % of the CO₂ in thewaste gas stream 311 is separated into the liquid CO₂ product stream.Separated CO₂ is removed in CO₂ stream 312. The remaining vapor phasematerials exit the low temperature separation unit 409 in vapor phasestream 313.

The vapor phase stream 313 from the low temperature separation unit 409can be recycled for a variety of uses. In FIG. 2, the vapor phase stream313 branches, and a first portion of the vapor phase passes in vaporphase portion one stream 314 through the heat exchanger 412 to combinewith the hydrocarbon feed stream 303. In this manner, the remainingimpurities are recycled back through the system, particularly being fedback into the GHR reactor 403.

In one or more embodiments, the hydrogen production system can include acombined heat source that is separate from the H₂+CO synthesis gasgeneration reactor but that is configured to provide heat that can beprovided to one or more streams of the hydrogen production system toincrease efficiency thereof. Power production systems can beparticularly beneficial for providing a combined heat source. Inparticular, one or more exhaust streams formed in a power productionsystem can be a combined heat source in that heat can be taken therefromfor transfer to one or more streams in the hydrogen production system.

A particularly beneficial integration of power production and hydrogenproduction is the gas turbine combined cycle power system. These unitsare used worldwide usually with natural gas as the fuel. The industrialgas turbine exhaust which is generally at a temperature in the range550° C. to 650° C. is passed through a large finned tube economizer heatexchanger where it is used to generate high pressure intermediatepressure and low pressure steam for additional power generation usingsteam turbines. The turbine exhaust at high temperature is suited foruse as a combined heat source for addition of heat to the hydrogenproduction system. Said combined heat source can be used, for example,for preheating the feed streams to the H₂ plant syngas reactors. Suchheating can be in the range of about 400° C. to about 1000° C., about425° C. to about 800° C., about 450° C. to about 600° C., or about 500°C. to about 550° C. Additionally, the excess heat available from the H₂plant is ideal for boiler feed-water preheating over a temperature rangeup to 400° C., which releases extra steam for power production in thesteam turbines. The main benefit lies in the use of the hydrogen as afuel in the gas turbine.

In systems and methods as described herein, the use of substantiallypure oxygen in the hydrogen plant syngas reactors can have the sidebenefit of providing a large quantity of substantially pure nitrogen asa by-product from the cryogenic air separation plant. The nitrogen canbe provided at relatively high pressure directly from the air separationunit as stream 93. At least a portion of this nitrogen can be blendedwith the hydrogen that can be produced as described herein. The endresult is an H₂+N₂ fuel gas that is suitable for use in a conventionalgas turbine combined cycle power generation system. The blended inertnitrogen is generally required to reduce the adiabatic flame temperaturein the gas turbine combustor and has the added benefit of increasing themass flow of gas in the power turbine. It can also be beneficial topreheat the H₂+N₂ fuel gas and add steam generated from the heat presentin the excess boiler feed water stream 59 at a temperature level below400° C.

The H₂+N₂ fuel gas can be utilized in any gas turbine combined cyclepower generation system. Known systems can be modified as necessary toremove, decommission, or otherwise forego the use of elements that wouldotherwise be required for removal of CO₂. Known gas turbine combinedcycle power generation systems that can be utilized according to thepresent disclosure are described in U.S. Pat. Nos. 8,726,628, 8,671,688,8,375,723, 7,950,239, 7,908,842, 7,611,676, 7,574,855, 7,089,727,6,966,171, and 6,474,069, the disclosures of which are incorporatedherein by reference.

The combination of H₂ production with 100% potential CO₂ capture with agas turbine combined cycle power generation system using at least aportion of the produced H₂ as fuel provided by the present disclosureresults in substantially no atmospheric discharge of CO₂ from thecombined system. This provides a distinct advantage over theconventional operation of a gas turbine combined cycle system. Inparticular, the present combination of systems can eliminate the naturalgas fuel typically required in a gas turbine and substitute a fuel withno CO₂ production when combusted. As such, in some embodiments, thepresent disclosure provides a combination of: 1) an oxygen basedhydrogen production unit with near 100% CO₂ capture; 2) a conventionalgas turbine combined cycle power generation unit using H₂+N₂ fuel gasthat provides power generation with zero CO₂ emission. The combinedsystem as described herein can provide a surprisingly high efficiency,low cost power generation, and approximately 100% CO₂ capture.

The combination of systems can be implemented in a variety of manners.In some embodiments, an existing combined cycle power station can beconverted to eliminate all CO₂ emissions and simultaneously increase thepower generation capacity. Such conversion can include addition of thefurther system components described herein for production of power usinga CO₂ circulating fluid and production of H₂+N₂ fuel gas.

As illustrated in FIG. 2, a gas turbine 410 is provided, and hydrocarbonfuel stream 321 is input thereto for combustion to produce power ingenerator 417. The gas turbine exhaust stream 322 is passed through theheat exchanger 412 to provide heating to hydrocarbon fuel stream 321,stream 401, stream 317, and stream 319. The temperature of the exhauststream 322 from the gas turbine 410 can be optionally raised by means ofduct-burning using, for example, fresh pre-heated natural gas taken fromstream 321 and input to stream 322, or using a waste fuel stream, suchas a vapor phase portion two stream 336 taken from stream 313 exitingthe low temperature CO₂ separation unit and input to stream 322. This isbeneficial to accommodate for required heating duty in the processheater 412, and the duct-burning thus can take place in the piping forstream 322. In some embodiments, streams 336 and 314 may be separatestreams exiting the low temperature CO₂ separation unit instead of beingbranches of a single exit stream, as illustrated.

In some embodiments, a hydrogen production facility as described hereincan be particularly suited to provide excess low temperature level heatthat can be used in a variety of further systems for a variety offurther reasons.

The waste gas from the PSA of the hydrogen production system can becompressed to typically about 200 bar to about 400 bar and mixed withthe feed hydrocarbon fuel used in a combustor of a power productionsystem. The waste gas contains not only flammable components CH₄+CO+H₂but also all the CO₂ produced in the H₂ production system. Alternativelythe waste gas from the PSA can be compressed to the inlet pressure ofthe first PSA, the CO₂ can be removed in one of a number of processesdescribed above, and the CO₂ depleted gas stream can be sent to a secondPSA to separate more H₂ to add to the total H₂ product stream.Optionally the waste gas can be preheated in an economizer heatexchanger, steam can be added and more H₂ can be produced in anadditional catalytic CO shift reactor, the gas can then be cooled in theeconomizer heat exchanger before being processed to separate more H₂ inthe second PSA. The hydrogen production system is thus suited forproduction of a significant quantity of low grade heat from the coolingH₂+CO stream at a temperature level of typically below 400° C. andpreferably in the range 240° C. to about 290° C.

Many modifications and other embodiments of the presently disclosedsubject matter will come to mind to one skilled in the art to which thissubject matter pertains having the benefit of the teachings presented inthe foregoing descriptions and the associated drawings. Therefore, it isto be understood that the present disclosure is not to be limited to thespecific embodiments described herein and that modifications and otherembodiments are intended to be included within the scope of the appendedclaims. Although specific terms are employed herein, they are used in ageneric and descriptive sense only and not for purposes of limitation.

1-24. (canceled)
 25. A carbon dioxide (CO₂) separation systemcomprising: a compressor configured for compressing a process stream,wherein the process stream comprises CO₂ and one or more furthercomponents; a drier configured for removing moisture from the processstream; at least one heat exchanger configured for cooling the processstream against one or more cooling streams and providing the processstream as a two-phase stream; at least one expander configured forcooling the two-phase stream via expansion of the two-phase stream; anda mass transfer column configured to receive the two phase stream andgenerate a vapor phase stream and a liquid phase stream.
 26. A hydrogenproduction system comprising: a reactor unit configured for receiving ahydrocarbon feed stream and oxygen and forming a product gas streamcomprising H₂+CO; a steam generating boiler configured for cooling theproduct gas stream comprising H₂+CO and for forming steam; at least onereactor configured for receiving the product gas stream comprising H₂+COand providing a stream comprising H₂+CO₂; a pressure swing adsorberconfigured to receive the stream comprising H₂+CO₂ and provide a productstream formed of substantially pure hydrogen and also provide waste gassteam comprising CO₂; a compressor configured for compressing the wastegas stream comprising the CO₂; a drier configured for removing moisturefrom the waste gas stream comprising the CO₂; at least one heatexchanger configured for cooling the waste gas stream comprising the CO₂against one or more cooling streams and providing the waste gas streamcomprising the CO₂ as a two-phase stream; at least one expanderconfigured for cooling the two-phase stream via expansion of thetwo-phase stream; and a separator configured for separating thetwo-phase stream into a vapor phase stream and a liquid phase stream.27. The hydrogen production system of claim 26, further comprising oneor more heat exchangers configured for heating the hydrocarbon feedstream against one or both of the product gas stream comprising H₂+COand the stream comprising H₂+CO₂.
 28. The hydrogen production system ofclaim 26, further comprising one or more heat exchangers configured fortransfer of excess heat to an external process.
 29. The hydrogenproduction system of claim 26, further comprising one or more linesconfigured for output of one or both of a waste fuel gas stream andsteam generated in the hydrogen production system.
 30. The hydrogenproduction system of claim 26, further comprising one or more linesconfigured for delivery of at least part of the product stream formed ofsubstantially pure hydrogen as fuel to a gas turbine.
 31. The hydrogenproduction system of claim 26, wherein the reactor unit comprises asteam plus hydrocarbon plus optionally CO₂ catalytic reformer.
 32. Thehydrogen production system of claim 26, wherein the reactor unitcomprises a partial oxidation unit.
 33. The hydrogen production systemof claim 26, wherein which the reactor unit comprises a catalyticauto-thermal reformer.
 34. The hydrogen production system of claim 26,wherein which the reactor unit comprises a first stage unit that iseither an auto-thermal reformer or a partial oxidation reactor andcomprises a second stage gas heated steam plus hydrocarbon catalyticreformer.
 35. The hydrogen production system of claim 26, wherein atleast part of the H₂+CO stream produced from the reactor unit isgenerated in an ITM partial oxidation reactor using a low pressurepreheated feed air stream air stream.
 36. The hydrogen production systemof claim 26, further comprising a super-heater heat exchanger configuredto transfer heat from an external heat source to at least thehydrocarbon feed stream.
 37. The hydrogen production system of claim 26,wherein the reactor unit is a combined pressure vessel comprised of apartial oxidation zone and a gas heated reformer.
 38. The hydrogenproduction system of claim 37, wherein the partial oxidation zone is ata bottom portion of the combined pressure vessel, and the gas heatedreformer comprises open-ended tubes in a middle zone of the combinedpressure vessel and a waste heat boiler heat exchanger at a top portionof the combined pressure vessel.
 39. A process for hydrogen production,the process comprising: reacting a hydrocarbon feed stream and oxygeninto a reactor unit to form a product gas stream comprising H₂+CO;passing the product gas stream comprising H₂+CO through a steamgenerating boiler to add steam to the product gas stream comprisingH₂+CO; converting the product gas stream comprising H₂+CO in at leastone reactor to form a stream comprising H₂+CO₂; processing the streamcomprising H₂+CO₂ in a pressure swing adsorber to provide a productstream formed of substantially pure hydrogen and also provide waste gassteam comprising CO₂; forming a liquid CO₂ product stream in a cryogenicseparation unit operating with auto-refrigeration by passing the wastegas stream comprising CO₂ therethrough such that at least 50 mol % ofthe CO₂ in the waste gas stream comprising CO₂ is separated into theliquid CO₂ product stream; and recycling a vapor phase stream from thecryogenic separation unit. 40-51. (canceled)